A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078698



Internal ID19324023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1249306..1314507hg38UCSC Ensembl
chrY:1318199..1383400hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3865202
hg1965202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768470
SamplesKWP1
Known GenesCSF2RA, MIR3690, MIR3690-2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078698
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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